A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18167390



Internal ID20734430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:142980529..142982712hg38UCSC Ensembl
chr8:144061946..144064129hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg382184
hg192184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6422998
Supporting Variants
Samples
Known GenesLOC100133669
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18167390
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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